Whiteman P - Search Results

1

Defective secretion of recombinant fragments of fibrillin-1: implications of protein misfolding for the pathogenesis of Marfan syndrome and related disorders.

Whiteman P, Handford PA. Whiteman P, et al. Hum Mol Genet. 2003 Apr 1;12(7):727-37. doi: 10.1093/hmg/ddg081. Hum Mol Genet. 2003. PMID: 12651868

2

A Gly --> Ser change causes defective folding in vitro of calcium-binding epidermal growth factor-like domains from factor IX and fibrillin-1.

Whiteman P, Downing AK, Smallridge R, Winship PR, Handford PA. Whiteman P, et al. J Biol Chem. 1998 Apr 3;273(14):7807-13. doi: 10.1074/jbc.273.14.7807. J Biol Chem. 1998. PMID: 9525872 Free article.

3

NMR analysis of cbEGF domains gives new insights into the structural consequences of a P1148A substitution in fibrillin-1.

Whiteman P, Downing AK, Handford PA. Whiteman P, et al. Protein Eng. 1998 Nov;11(11):957-9. doi: 10.1093/protein/11.11.957. Protein Eng. 1998. PMID: 9876915

4

EGF-like domain calcium affinity modulated by N-terminal domain linkage in human fibrillin-1.

Smallridge RS, Whiteman P, Doering K, Handford PA, Downing AK. Smallridge RS, et al. Among authors: whiteman p. J Mol Biol. 1999 Feb 26;286(3):661-8. doi: 10.1006/jmbi.1998.2536. J Mol Biol. 1999. PMID: 10024441

5

A G1127S change in calcium-binding epidermal growth factor-like domain 13 of human fibrillin-1 causes short range conformational effects.

Whiteman P, Smallridge RS, Knott V, Cordle JJ, Downing AK, Handford PA. Whiteman P, et al. J Biol Chem. 2001 May 18;276(20):17156-62. doi: 10.1074/jbc.M006547200. Epub 2001 Jan 31. J Biol Chem. 2001. PMID: 11278305 Free article.

6

Solution structure and dynamics of a calcium binding epidermal growth factor-like domain pair from the neonatal region of human fibrillin-1.

Smallridge RS, Whiteman P, Werner JM, Campbell ID, Handford PA, Downing AK. Smallridge RS, et al. Among authors: whiteman p. J Biol Chem. 2003 Apr 4;278(14):12199-206. doi: 10.1074/jbc.M208266200. Epub 2003 Jan 2. J Biol Chem. 2003. PMID: 12511552 Free article.

7

Structural consequences of cysteine substitutions C1977Y and C1977R in calcium-binding epidermal growth factor-like domain 30 of human fibrillin-1.

Suk JY, Jensen S, McGettrick A, Willis AC, Whiteman P, Redfield C, Handford PA. Suk JY, et al. Among authors: whiteman p. J Biol Chem. 2004 Dec 3;279(49):51258-65. doi: 10.1074/jbc.M408156200. Epub 2004 Sep 14. J Biol Chem. 2004. PMID: 15371449 Free article.

8

The molecular genetics of Marfan syndrome and related disorders.

Robinson PN, Arteaga-Solis E, Baldock C, Collod-Béroud G, Booms P, De Paepe A, Dietz HC, Guo G, Handford PA, Judge DP, Kielty CM, Loeys B, Milewicz DM, Ney A, Ramirez F, Reinhardt DP, Tiedemann K, Whiteman P, Godfrey M. Robinson PN, et al. Among authors: whiteman p. J Med Genet. 2006 Oct;43(10):769-87. doi: 10.1136/jmg.2005.039669. Epub 2006 Mar 29. J Med Genet. 2006. PMID: 16571647 Free PMC article. Review.

9

Fibrillin-1 misfolding and disease.

Whiteman P, Hutchinson S, Handford PA. Whiteman P, et al. Antioxid Redox Signal. 2006 Mar-Apr;8(3-4):338-46. doi: 10.1089/ars.2006.8.338. Antioxid Redox Signal. 2006. PMID: 16677079 Review.

10

Cellular and molecular studies of Marfan syndrome mutations identify co-operative protein folding in the cbEGF12-13 region of fibrillin-1.

Whiteman P, Willis AC, Warner A, Brown J, Redfield C, Handford PA. Whiteman P, et al. Hum Mol Genet. 2007 Apr 15;16(8):907-18. doi: 10.1093/hmg/ddm035. Epub 2007 Feb 26. Hum Mol Genet. 2007. PMID: 17324963

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